ClinGen Allele Registry
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Canonical Allele Identifier:
PA645497883
Gene: HSD17B10
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000484484
RCV000623879
RCV001755724
RCV002274038
ClinVar Variation:
420778
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004484.1:p.Arg147Cys
CA16621449
NM_004493.3:c.439C>T